Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The relationships between FAM5C SNP (rs10920501) variability and metabolic syndrome and inflammation in women with coronary heart disease.

Biological research for nursing - 1 Apr 2013

Cline Jennifer L, Beckie Theresa M

Abstract excerpt

INTRODUCTION: The leading cause of death among women is coronary heart disease (CHD), a multifactorial disease with polygenic heritability estimated at 50%. Polymorphisms in the family with sequence similarity 5, member C' (FAM5C) gene have been associated with myocardial infarction (MI). FAM5C also corresponds directly with the inflammatory biomarker monocyte chemoattractant protein 1 (MCP-1) and metabolic...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Aged
Share to Aged, 80 and over
Share to Coronary Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Inflammation

Share to Metabolic Syndrome

Share to Polymorphism, Single Nucleotide

Source

Open in PubMed Open full text

Identifiers

PMID: 22013132
DOI: 10.1177/1099800411424487
PMCID: PMC4108984

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The relationships between FAM5C SNP (rs10920501) variability and metabolic syndrome and inflammation in women with coronary heart disease.PMID 22013132Read ↗

Genetic and functional association of FAM5C with myocardial infarction.Semantic proximity Read ↗

Common and Rare Genetic Variation in CCR2, CCR5, or CX3CR1 and Risk of Atherosclerotic Coronary Heart Disease and Glucometabolic Traits.Semantic proximity Read ↗

Association of the PSRC1 rs599839 Variant with Coronary Artery Disease in a Mexican Population.Semantic proximity Read ↗

Allele-Specific Epigenetic Regulation of FURIN Expression at a Coronary Artery Disease Susceptibility Locus.Semantic proximity Read ↗

Interferon Regulatory Factor 5 (IRF5) Gene Haplotypes Are Associated with Premature Coronary Artery Disease. Association of the IRF5 Polymorphisms with Cardiometabolic Parameters. The Genetics of Atherosclerotic Disease (GEA) Mexican Study.Semantic proximity Read ↗

Allele-specific epigenetic regulation of <i>FURIN</i> expression at a coronary artery disease susceptibility locusSemantic proximity Read ↗

Association of FKBP5 genotype with depressive symptoms in patients with coronary heart disease: a prospective study.Semantic proximity Read ↗

The (G>A) rs11573191 polymorphism of PLA2G5 gene is associated with premature coronary artery disease in the Mexican Mestizo population: the genetics of atherosclerotic disease Mexican study.Semantic proximity Read ↗

Macrophage migration inhibitory factor promoter polymorphisms (-794 CATT5-8): Relationship with soluble MIF levels in coronary atherosclerotic disease subjects.Semantic proximity Read ↗

Correlation analysis between ApoM gene-promoter polymorphisms and coronary heart disease.Semantic proximity Read ↗

Polymorphism rs7023923 and monocyte count in blood donors and coronary artery disease patients.Semantic proximity Read ↗

FURIN Expression in Vascular Endothelial Cells Is Modulated by a Coronary Artery Disease-Associated Genetic Variant and Influences Monocyte Transendothelial Migration.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.